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NCT Number: NCT07659691

Multisensory Rehabilitation of Vision Loss After Cortical Damage

Damage to visual cortex on one side of the brain frequently produces a profound and permanent blindness in contralesional space (hemianopia), a debilitating condition that causes enormous suffering for patients and their families.

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Wake Forest University Health Sciences

Winston-Salem, North Carolina, 27157, United States

Location contact

Wendy Jenkins, BSNRN, CCRC

CONTACT

[email protected]

336-716-3842

About this study

The over-arching objective of the current proposal is to evaluate the functional recovery of vision in hemianopic (blindness in one hemifield) and quadrantanopic (blindness in one quadrant) patients engaged with a multisensory training paradigm. This will pave the way for clinical trials in which this simple, non-invasive training paradigm can be developed for therapeutic use to treat blindness resulting from cortical damage.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients will be recruited from the local subject population hospitalized/seen by Ophthalmology, Neurosurgery, and Neurology at Atrium Health Wake Forest Baptist
  • diagnosis of stable homonymous hemianopia (>4 weeks) with absence of hemineglect
  • a lesion encompassing at least primary visual cortex but sparing parietal cortex, to include lesions caused by an ischemic or hemorrhagic stroke or post-surgical changes due to an oncologic or non-oncologic tumor
  • normal or correctable auditory and cognitive function
  • willingness to participate in the three-month program
  • ability to perform visual discriminations in their intact field
  • life expectancy ≥12 months

Exclusion criteria

  • diagnosis of an unstable homonymous hemianopia and/or with hemineglect,
  • Abnormal or uncorrectable auditory and cognitive function
  • unwillingness to participate in the program
  • inability to perform the visual testing in their intact field
  • life expectancy < 12 months
  • Any other condition that would compromise their ability to complete the study.

Treatment and study plan

Multisensory Rehabilitation

Behavioral

12 research sessions + clinical visits at the time of the first and last session - In each session, there will be a "training phase" in which subjects will be exposed (and respond) to spatiotemporally congruent pairs of visual-auditory stimuli presented within their blinded field, with occasional probes of unisensory visual stimuli on both sides of space. There will also be a "testing" phase during which they are presented with visual stimuli in virtual reality (VR) to assess multiple aspects of visual function. This "visual battery" consists of innocuous stimuli, e.g., flashes of light or moving bars, presented at intensities consistent with those experienced during daily life. Subjects detect or discriminate the stimuli (e.g., judge whether a stimulus was flashed, or which stimulus is brighter) and report confidence in assessments.

Other names: multisensory training paradigm

Primary outcomes

  1. Change in National Institutes of Health Stroke Scale (NIHSS) score

    Time frame: Month 6

    The National Institutes of Health Stroke Scale (NIHSS) is a standardized, 15-item physical and mental examination used by healthcare providers to objectively quantify the severity of an acute stroke. Scores range from 0 (no neurological deficit) to 42 (severe impairment).

  2. Change in Activity Inventory scores

    Time frame: Month 6

    A questionnaire that asks how vision affects everyday activities. It helps show which daily tasks are most important to the participant and how difficult those tasks may be because of vision problems. Patients rate the importance of a goal and the difficulty of tasks, resulting in an individually tailored dataset. This adaptive approach provides a comprehensive profile of how visual limitations affect everyday life.

Study contacts

Contact information is provided by the study sponsor or research team.

Kimberly Hawley, RN

CONTACT

[email protected]

3367164031

Wendy Jenkins, BSNRN, CCRC

CONTACT

[email protected]

336.716.3842

Sponsors and collaborators

Lead sponsor

Wake Forest University Health Sciences

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jun 22, 2026
Registry last updated
Jun 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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